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Thermo Fisher Scientific CSH1 Monoclonal Antibody (OTI2G4), TrueMAB
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Thermo Fisher Scientific CSH1 Monoclonal Antibody (OTI2G4), TrueMAB

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CSH1 단백질을 인식하는 Mouse monoclonal antibody로, Western blot과 IHC(P) 검증 완료. Lyophilized 형태로 제공되며, PBS buffer(8% trehalose)에 보관. 인체 CSH1 단백질 연구용으로 적합하며, 재구성 및 컨주게이션 실험에 용이.

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마지막 업데이트 2025. 08. 02. 오후 05:39
Thermo Fisher Scientific CF506708 CSH1 Monoclonal Antibody (OTI2G4), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific CSH1 Monoclonal Antibody (OTI2G4), TrueMAB

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:150

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone OTI2G4
Immunogen Full length human recombinant protein of human CSH1 produced in HEK293T cells
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, add 100 µL of distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using this carrier-free antibody, perform an additional desalting step (Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).

Target Information

The protein encoded by the CSH1 gene belongs to the somatotropin/prolactin family of hormones and plays a key role in growth control.
This gene is located at the growth hormone locus on chromosome 17, together with four related genes in the same transcriptional orientation, likely evolved through gene duplication.
Although these five genes share high sequence identity, they are selectively expressed in different tissues.
Alternative splicing generates additional isoforms, increasing diversity and functional specialization.
CSH1 is mainly expressed in the placenta and utilizes multiple transcription initiation sites.
Mutations in this gene are associated with placental lactogen deficiency and Silver-Russell syndrome.


For Research Use Only.
Not for use in diagnostic procedures. Not for resale without express authorization.

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